Disease

Binge Eating Disorder

About the Disease
Bulimia Nervosa, also known as bulimia, is related to abdominal obesity-metabolic syndrome 1 and polysubstance abuse, and has symptoms including salt craving, symptoms and decrease in appetite. An important gene associated with Bulimia Nervosa is BULN (Bulimia Nervosa, Susceptibility To), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. The drugs Memantine and Sibutramine have been mentioned in the context of this disorder. Affiliated tissues include thyroid, prefrontal cortex and skin, and related phenotypes are bulimia and nervous system

Common Targets
Carbonic Anhydrase (nonspecified subtype) | BDNF | GPR139 | 5-Hydroxytryptamine Receptor 3 (5-HT3 receptor) (nonspecified subtype) | G7099 | CACNA2D1 | OPRK1 | GHSR | Kainate Receptor (GluR) (nonspecified subtype) | OPRM1 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | Gamma-Aminobutyric acid type B receptor | DRD2 | SIGMAR1 | Alpha-2 Adrenergic receptors (nonspecified subtype) | T-Type Calcium Channel | HTR1A | CRH | SLC6A2 | ANKK1 | HCRTR1 | LINC00880 | Glutamate Transporter (nonspecified subtype) | SLC44A3-AS1 | LINC01260 | FLNA | Voltage-Gated Sodium Channel Complex | OXT | ARHGAP8 | OPRD1 | PRR5-ARHGAP8 | NPY5R | Sodium channel (nonspecified subtype) | HCRTR2 | BDNF-AS | FASN | SLC6A4 | ANG | CRHR1 | NMDA receptor | CA2 | RNASE4 | HTR2A | SLC5A1 | HTR1B | DAGLA | alpha1-Adrenoceptor (nonspecified subtype) | FTO | 5-Hydroxytryptamine Receptor (nonspecified subtype) | PNLIP | DRD3 | ANK2 | PNOC | GLP1R | SLC6A3 | OXTR | TAAR1 | CLOCK | HTR1D | HTR7 | ENPP2 | Glutamate Receptor Ionotropic AMPA Receptor | NRXN3 | LIPF

疾病靶点研报
Binge Eating Disorder

Note: If you'd like to get a target analysis report for Binge Eating Disorder, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Binge Eating Disorder at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Photosensitivity | Carbohydrate Metabolism Disorders | Spinocerebellar Ataxia Type 3 | Hemochromatosis Type 1 | Keratosis, Actinic | Mycosis Fungoides | Bethlem Myopathy | Meniere's Disease | Syndactyly | Uveitis, Anterior | Autosomal Recessive Spastic Paraplegia Type 35 | Congenital Lipoid Adrenal Hyperplasia | Achromatopsia | Acute Anterior Uveitis | Chronic Inflammatory Demyelinating Polyneuropathy | Spermatocele | Neurodegeneration With Brain Iron Accumulation | Cri-du-chat Syndrome | Schnitzler Syndrome | POEMS Syndrome | Exocrine Pancreatic Insufficiency | Central Core Disease | Multiple Epiphyseal Dysplasia | Atelosteogenesis Type 2 | Congenital Primary Aphakia | Non-small Cell Lung Cancer | Spitzoid Melanoma | Basan Syndrome | Multiple Hamartoma Syndrome | Juvenile Polyposis | Pityriasis Rubra Pilaris | Hemorrhagic Disorders | Multiple Myeloma | Retinal Vasculitis | Temporal Lobe Epilepsy | Familial Male-limited Precocious Puberty | Adenocarcinoma | Keratoconjunctivitis | Multiple Sclerosis, Primary Progressive | Alazami Syndrome | Nasodigitoacoustic Syndrome | Tendinitis | Chronic Myelomonocytic Leukemia | Lassa Fever | Still Disease | Pyoderma Gangrenosum | Optic Neuropathy, Anterior Ischemic | Primary Progressive Nonfluent Aphasia | Cluster Headache | Eccrine Porocarcinoma | Ornithine Transcarbamylase Deficiency | B-cell Prolymphocytic Leukemia | Thalassemia | Erythematotelangiectatic Rosacea | Lymphangiomatosis | Retinitis | Dermatofibrosarcoma | Lewy Body Dementia | Urea Cycle Disorder | Adenoma, Pleomorphic | Urofacial Syndrome | Hyperlipidemia Type V | Acute Kidney Injury | Glycogen Storage Disease Type 1b | Glutathione Synthetase Deficiency | Exotropia | Conduct Disorder | Keratosis | Dystrophy, Cone-rod | Microcephaly | Restrictive Dermopathy | Takayasu's Arteritis | Sialoadenitis | Glycogen Storage Disease Type 1 | Autonomic Nervous System Disorders | Sclerosing Cholangitis | Primary Carnitine Deficiency | Keratitis-ichthyosis-deafness Syndrome | Tangier Disease | Coffin-Siris Syndrome | Hemochromatosis Type 2 | Parvovirus B19 Infection | Heterotaxy | Tuberculosis | Isobutyryl-CoA Dehydrogenase Deficiency | Plasmacytoma | Gout | Sleep Apnea, Obstructive | Epidermal Nevus Syndrome | Neurocutaneous Syndromes | Ganglioneuroma | Pneumonia, Viral | Rhinitis | Persistent Mullerian Duct Syndrome | Hypoproteinemia, Hypercatabolic | Nail-Patella Syndrome | Polycystic Ovary Syndrome | Paraganglioma | FG Syndrome | Best Macular Dystrophy | Pemphigus | Myoclonic Epilepsy With Ragged Red Fibers | Osteomalacia | Atelosteogenesis Type 1 | Hereditary Pyropoikilocytosis | Glioblastoma Multiforme | Hemophilia | Chloridorrhea, Congenital | Carney-Stratakis Syndrome | Glomerulonephritis | Premature Ejaculation | Familial Hemiplegic Migraine | Delirium | Bulimia Nervosa | Irritable Bowel Syndrome | Arthritis | Meckel-Gruber Syndrome | Hypercholesterolemia | Porphyria, Acute Intermittent | Malonyl-CoA Decarboxylase Deficiency | Primary Biliary Cholangitis | Metachromatic Leukodystrophy | Gastroenteritis | Narcolepsy | Generalized Epilepsy With Febrile Seizures Plus | Fetal And Neonatal Alloimmune Thrombocytopenia | Kidney Stones | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | D-2-Hydroxyglutaric Aciduria | Urethritis | Heart Septal Defects | Anuria | Axenfeld-Rieger Syndrome | Multiple Sclerosis, Secondary Progressive | Epilepsy, Generalized | Brenner Tumor | Allergic Contact Dermatitis | Hyperandrogenemia | Hodgkin Lymphoma | Early Infantile Epileptic Encephalopathy 4 | Veno-occlusive Disease | 3-hydroxy-3-methylglutaric Aciduria | Synpolydactyly | Diarrhea | Juvenile Xanthogranuloma | Christianson Syndrome | Erectile Dysfunction | Stargardt Disease | Pachyonychia Congenita | Hypertension, Portal | Sclerosteosis | Bone Giant Cell Tumor | Portal Vein Thrombosis | Schwannoma | Behavioral Variant Of Frontotemporal Dementia | Bartter Syndrome | Glycogen Storage Disease Type 1a | Cardiomyopathy, Hypertrophic | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Periodic Limb Movement Disorder | Spinocerebellar Ataxia Type 2 | Lupus Erythematosus | Trichuriasis | Usher Syndrome Type I | Spondylo-ocular Syndrome | Diabetes Type 2 | Sarcoma, Alveolar Soft Part | Apparent Mineralocorticoid Excess Syndrome | Feingold Syndrome | Hypersomnia | Arts Syndrome | Microcephaly, Seizures, And Developmental Delay | Distal Myopathy | Congenital Muscular Dystrophy | Lactose Intolerance | Esophageal Motility Disorders | Dyskeratosis Congenita | Cold Agglutinin Disease | Cole-Carpenter Syndrome | Recurrent Respiratory Papillomatosis | KBG Syndrome | Cholangiocarcinoma | Combined Malonic And Methylmalonic Acidemia | Patent Foramen Ovale | Paroxysmal Nocturnal Hemoglobinuria | Metabolic Diseases | Triphalangeal Thumb-polysyndactyly Syndrome | Nance-Horan Syndrome | Mitochondrial DNA Depletion Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Leiomyoma | Familial Retinal Arterial Macroaneurysm | Osteogenesis Imperfecta Type II | Astigmatism | Polyarteritis Nodosa | Hypertrophy | Pulmonary Tuberculosis | Pontocerebellar Hypoplasia | Early Infantile Epileptic Encephalopathy 1 | Chediak-Higashi Syndrome | Neuroma | Waardenburg Syndrome | Androgenic Alopecia | Retinoschisis | Dengue Shock Syndrome | Erythema Multiforme | Hereditary Spastic Paraplegia | Azoospermia | Peritonitis | Adenosine Deaminase 2 Deficiency | Cerebral Amyloid Angiopathy | Basal Ganglia Disease | Personality Disorders | Megalencephaly | Neurodevelopmental Disorders | Borderline Personality Disorder | Neonatal Progeroid Syndrome | X-linked Creatine Transporter Deficiency | Autoimmune Disease | Epidermodysplasia Verruciformis | Generalized Epilepsy And Paroxysmal Dyskinesia | Multiple Sclerosis | Stomatitis | Eosinophilia | Argininosuccinic Aciduria | Hepatoblastoma | Congenital Sodium Diarrhea | Hypercholesterolemia, Familial | Brugada Syndrome 1 | Majeed Syndrome | Malignant Fibrous Histiocytoma | Spinocerebellar Ataxia Type 27 | Fanconi Syndrome | Bronchitis, Chronic | Beckwith-Wiedemann Syndrome | Keloid | Juvenile Hyaline Fibromatosis | Gastritis | Macrophagic Myofasciitis | Familial Hypertrophic Cardiomyopathy | Gastroschisis | Glaucomatocyclitic Crisis | Seborrheic Dermatitis | Macrodactyly | Hypertriglyceridemia | Optic Neuropathy | Epidermolytic Ichthyosis, Annular | Craniometaphyseal Dysplasia | Cousin Syndrome | Sickle Cell Anemia | Protein S Deficiency | Toxoplasmosis | Mucolipidosis Type II | Sensory Neuropathy | Porphyria Cutanea Tarda | Saul-Wilson Syndrome | Pigment Dispersion Syndrome | Hypotrichosis | Polyomavirus Nephropathy | Intestinal Obstruction | Ichthyosis Hystrix, Curth-Macklin Type | Walker-Warburg Syndrome | Ameloblastoma | Hyperparathyroidism | Cholecystitis | Chordoma | Chromosome 8q21.11 Deletion Syndrome | Inflammatory Joint Disease | Krabbe Disease | Osteogenesis Imperfecta Type V | Idiopathic Multicentric Castleman Disease | McKusick Type Metaphyseal Chondrodysplasia | Enhanced S-cone Syndrome | Epidermolytic Palmoplantar Keratoderma | DOCK8 Immunodeficiency Syndrome | Tonsillitis | Ichthyosis Bullosa Of Siemens | Megaloblastic Anemia | Bardet-Biedl Syndrome | Hyperammonemia | Familial Exudative Vitreoretinopathy | Osteogenesis Imperfecta Type I | Hemolytic Uremic Syndrome | Gynecomastia | Papillorenal Syndrome | Loeys-Dietz Syndrome Type 4 | Chromosome 17q21.31 Deletion Syndrome | Ocular Surface Squamous Neoplasia | Glycogen Storage Disease Type 0, Muscle | Polymicrogyria | Ophthalmoplegia | Polyneuropathy | Eosinophilic Asthma | Haim-Munk Syndrome | Encephalopathy, Ethylmalonic | Contact Dermatitis | Amblyopia | Mucolipidosis | Pyruvate Dehydrogenase Deficiency | Nemaline Myopathy 8 | Neuropathy | Hepatitis, Chronic | Lymphoma | Desmosterolosis | Cancer, Bladder | Hemolytic Uremic Syndrome, Atypical | Cenani-Lenz Syndactyly Syndrome | GATA2 Deficiency | Norrie Disease | Fibrodysplasia Ossificans Progressiva | Acromegaly | Distal Spinal Muscular Atrophy | Facioscapulohumeral Muscular Dystrophy | Maternally Inherited Diabetes And Deafness | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Chordoid Glioma | Paracoccidioidomycosis | Congenital Dyserythropoietic Anemia | Dwarfism | Bronchiectasis | Desbuquois Syndrome | Aneurysm, Abdominal Aortic | Ileitis | Vitreoretinal Degeneration, Snowflake Type | Tyrosine Hydroxylase Deficiency | Zellweger Syndrome | Peeling Skin Syndrome Type B | Primary Hyperoxaluria Type 3 | Pregnancy, Ectopic | Spinocerebellar Ataxia Type 16 | Osteoporosis-pseudoglioma Syndrome | Hemoglobinopathies | Cataplexy | Gastritis, Atrophic | Seizures-scoliosis-macrocephaly Syndrome | Spinal And Bulbar Muscular Atrophy | Chylothorax, Congenital | Acute Tubular Necrosis | Fibromuscular Dysplasia | GLUT1 Deficiency Syndrome | Lichen Planus | Oculocutaneous Albinism | Scoliosis | Myocardial Infarction | Gray Platelet Syndrome | Keratosis, Seborrheic | Split Hand-foot Malformation | Osteosclerosis | Infantile Nephropathic Cystinosis | Malaria | Tumoral Calcinosis | Smoldering Myeloma | Plasma Cell Dyscrasia | Ehlers-Danlos Syndrome | Myofibromatosis | Campomelic Dysplasia | Hydronephrosis | Microvillus Inclusion Disease | Chronic Mucocutaneous Candidiasis | Schistosomiasis Mansoni | Homocystinuria | Multicentric Carpotarsal Osteolysis Syndrome | Alzheimer Disease, Late Onset | Spondylosis | Traboulsi Syndrome | Spinocerebellar Ataxia Type 8 | Coronary Restenosis | Osteitis | Colitis, Collagenous | Myoclonic Atonic Epilepsy | Heroin Dependence | Clouston Hidrotic Ectodermal Dysplasia | Chronic Idiopathic Myelofibrosis | Cocaine-Related Disorders | Sleep Apnea, Central | Hypogonadism | Giant Cell Arteritis | Heavy Chain Disease | Primary Sclerosing Cholangitis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | MELAS Syndrome | Cerebral Cavernous Malformations | Fibronectin Glomerulopathy | Epithelioid Hemangioma | Prostatitis | Giant Axonal Neuropathy | Primary Pigmented Nodular Adrenocortical Disease | CREST Syndrome | Werner's Syndrome | N-acetylglutamate Synthase Deficiency | Spinocerebellar Ataxia Type 10 | Multicystic Renal Dysplasia | Blepharospasm | Chromosome 16p11.2 Deletion Syndrome | Reflex Epilepsy | Osteochondroma | Pyruvate Kinase Deficiency | Non-Hodgkin Lymphoma | Neutrophilia | Cervicitis